Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts

Wednesday, February 22, 2012

Lenten meditation

"those whom society sees as serving no purpose are often the ones closest to God because they recognize their dependence upon Him. Meanwhile, those traits which we admire most in ourselves and others—intelligence, wealth, self-reliance, common sense, respectability—become occasions for sin. They create barriers in our relationship with God because they become points of pride and prejudice. We shall have to give them up (or, at least, our reliance upon them) in order to enter the kingdom of God."
This lesson, culled by Jennifer Ferrara, the author of an amazing article in Godspy (remember that wonderful website?) is my theme for lessons in humility this Lent. To whom much is given, much is expected. I have been the recipient of many gifts, but pride can destroy my relationship with God and thus the source of my gifts is cut off. I will eventually run out of inspiration and wind down, but much time will be lost. My friend Dr Nadal talks about this in his Lenten meditation here.

On the night before Lent, it is a time for me to contemplate my own imperfections. As I contemplate them I think of how often my imperfections, my own shortcomings as a human being have enfolded me in paralyzing fear and guilt and have prevented me from becoming all I can be, all that God has called me to be. 
I see my calling as a writer and advocate to draw society's attention to those whom we often disregard, look down on or worst of all, think should not exist.  My goal is to remember myself that most of them are probably on line ahead of me to get into Heaven, with the people who annoy me at the local Walmart.
Read Jennifer Ferrara's meditation on "Revelation" a short story by Flannery O'Connor at the Godspy archives. 

Bookmark and Share

Tuesday, August 23, 2011

The Holy Father meets disabled children in Madrid

I wrote a few reflections on the poignant meeting of the Holy Father with disabled youth in Madrid. Its over at Catholic Vote.
Bookmark and Share

Wednesday, November 10, 2010

Autism gene found; will abortion follow?

A new marker has been found which indicates the possibility of autism and other impairments in an unborn baby. Will they soon be targeted for destruction like our children with Down syndrome children? Kurt Kondrich, author of "Making a Case for Life" asks this important question in his Renew America article.
The "risk gene" is identified as CNTNAP2, and according to the article "About one-third of all people carry the variant of the CNTNAP2 gene that is associated with a heightened risk of autism, as well as attention-deficit/hyperactivity disorder, Tourette syndrome, schizophrenia and other language difficulties." As I read this latest genetic update I noticed that the phrase "risk gene" was mentioned no fewer than 7 times.
Since 90%+ of all children diagnosed prenatally with Down syndrome using genetic testing are aborted my question to the researchers and medical community would be "What will the identification of this "risk gene" be used for, and will this prenatal diagnosis be offered to expectant parent?"

We hope not, but experience has taught us that those who view a perfect child as an entitlement will use this marker as a means to weed out imperfect children, decimating the Autim population. This has been the research goal of Autism Speaks, a well funded Autism organization.Look at this site; The Autism Genocide Clock, which estimates that in 4 years those with Autism will be targeted like our kids with Down syndrome are.
Bookmark and Share

Wednesday, January 27, 2010

Disability or profound gift?

There is a beautiful meditation on disabilities from Monsignor Charles Pope at the Archdiocese of Washington DC website.
 Over twenty years ago I worked for a year with the profoundly mentally disabled. They lay in beds and wheelchairs often with little muscle control. None of them could talk and only a few could engage in rudimentary communication. There was one man in his forties who had never emerged from the fetal position. He lay in a large crib his tiny yet clearly adult body curled up like a newborn babe. And on his face the most angelic smile that almost never diminished. He had been baptized as an infant and to my knowledge could not have sinned. I looked with marvel each visit upon innocence and a beatific countenance. What an astonishing gift he was. And who knows but God why he was this way? But God DOES know and had very important reasons. There was something central and indispensable in this man’s existence. Some role only he could fill. Apparently I was not able to fill that role. He was not disabled, he was differently abled, uniquely abled for something different than the ordinary. Looking upon him I had little doubt that he was directly in touch with God in a way that I never had been for his radiant face infallibly conveyed that. With our human eyes we can be saddened even appalled. But we’ll understand it better by an by. One day in the great by and by we may well be surprised to learn that the most central and critical people in God’s plan were the most humble and often the most broken and that we would never have made it without them.
Thank you Monsignor Pope for this profound meditation on the unfathomable gifts of a loving God. We are grateful that you see our children through the eyes of faith and that you are helping others to do the same. May God richly reward your efforts.

Bookmark and Share

Thursday, September 17, 2009

Rep Cathy McMorris Rogers supports Healthcare for Gunner

Rep Cathy McMorris Rogers is a champion for disabled children, as well as the proud mother of Cole, her son with Down syndrome. Here is a link to the YouTube video of her remarks at Healthcare for Gunner press conference yesterday.
Bookmark and Share

Wednesday, September 16, 2009

Healthcare for Gunner press conference in Washington DC

I was part of this group who spoke out about fears that our disabled children will be denied health care when resources dwindle, as they have in Canada.

Bookmark and Share

Wednesday, September 2, 2009

A short life full of love

Click here to see a documentary about a Texan couple who gave life to their son with Trisomy 13. See the love in this beautiful family and pray for those who made another choice out of despair.
NOTE: The film says that Trisomy 13 is always fatal but my research tells me that there are about 10-20% of children born with Trisomy 13 that live past the first year so disorder is not always immediately fatal. Each child is different.

Bookmark and Share

Wednesday, August 26, 2009

Will Obamacare be dangerous for Christina?

I think so.
Sarah Palin thinks so.
The family of Terri Schindler Schiavo think so.
Read the follow from the Terri Schindler Schiavo Foundation and see if you agree that the disabled may find themselves denied access to health care once cost-cutting becomes necessary.

"Was President Obama Subtly Promoting Euthanasia . . .?
Who is going to decide whether or not “you're better off” with or without the surgery? What about “additional tests” or “extra care”? Will it be your physician or will it be President Obama?

Recently, during a nationally televised event at the White House, President Obama said that families need better information so they don't unthinkingly approve, “additional tests or additional drugs that the evidence shows is not necessarily going to improve care.” He added: “Maybe you're better off not having the surgery, but taking the painkiller.”
Do we need any more evidence how this President and his administration feel about the equality and dignity of human life? It seems to be becoming more and more clear that if the quality of your life has reached the point where – by the judgment of a government official – your condition will no longer improve, the Obama health care plan will no longer allow any means of help. However, even more alarming is the real possibility of an Obama health care system that would seemingly put into practice an aggressive agenda to either hasten death or, worse yet, impose death on our cognitively disabled, chronically sick and frail."

I fear for my daughter Christina who has Down syndrome. I fear for her under Obamacare, once I am gone, some death panel will decide that her life is not of sufficient 'quality' to merit medical treatment. Tomorrow I will join pro-life activists Rev Pat Mahoney and Chris Slattery on Martha's Vineyard to tell President Obama about my concerns for my daughter.
I will update you on news coverage here.


Bookmark and Share

Monday, April 20, 2009

Susan Boyle; overcoming the tyranny of low expectations

As a mentally disabled schoolgirl with frizzy hair, Susan was mocked. She was one of 9 children, and lived with her parents caring for them till their deaths, she attended Sunday Mass and sang in the choir.Her life was one of quiet service.
I'd call her a success, just based on that. However, thanks to her triumph at "Britain's Got Talent" the world is calling her a success as well.
Why did they assume that she was a loser just because she doesn't fit the stereotype of a beautiful slim young vocalist?
If you are too loving to have been one of the crowd who laughed at Susan's dream, then this story will make your day, over at Aliens in this World blog.
UPDATE: I have the embedded video!!